Variant position: 391 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 890 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human DLWITMLSMIVGATCYAMFV GHATALIQSLDSSRRQYQEKY
Mouse DLWITMLSMIVGATCYAMFV GHATALIQSLDSSRRQYQEKY
Rat DLWITMLSMIVGATCYAMFV GHATALIQSLDSSRRQYQEKY
Rabbit DLWITMLSMIVGATCYAMFV GHATALIQSLDSSRRQYQEKY
Fission yeast -------------------- --TEEALQKNEESTRLSPEKK
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 890 Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
372 – 392 Helical; Name=Segment S6
369 – 400
Diagnostic targeted resequencing in 349 patients with drug-resistant pediatric epilepsies identifies causative mutations in 30 different genes.
Parrini E.; Marini C.; Mei D.; Galuppi A.; Cellini E.; Pucatti D.; Chiti L.; Rutigliano D.; Bianchini C.; Virdo S.; De Vita D.; Bigoni S.; Barba C.; Mari F.; Montomoli M.; Pisano T.; Rosati A.; Guerrini R.;
Hum. Mutat. 38:216-225(2017)
Cited for: VARIANTS EIEE24 ILE-153 AND ASP-391;
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